Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: INSC[original query] |
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Polymorphisms in the transforming growth factor beta 1 gene and osteoporosis. Bone 2003 Mar 32 (3): 297-310. Langdahl Bente Lomholt, Carstens Mette, Stenkjaer Liselotte, Eriksen Erik Fi |
Contribution of NTRK2 to the genetic susceptibility to anorexia nervosa, harm avoidance and minimum body mass index. Molecular psychiatry 2005 Sep 10 (9): 851-60. Ribases M, Gratacos M, Badia A, Jimenez L, Solano R, Vallejo J, Fernandez-Aranda F, Estivill |
Increased intestinal permeability and NOD2 variants in familial and sporadic Crohn's disease. Alimentary pharmacology & therapeutics 2006 May 23 (10): 1455-61. D'Incà R, Annese V, di Leo V, Latiano A, Quaino V, Abazia C, Vettorato M G, Sturniolo G |
Genetic susceptibility to tardive dyskinesia among schizophrenia subjects: IV. Role of dopaminergic pathway gene polymorphisms. Pharmacogenetics and genomics 2006 Feb 16 (2): 111-7. Srivastava Vibhuti, Varma Panchami G, Prasad Suman, Semwal Prachi, Nimgaonkar Vishwajit L, Lerer Bernard, Deshpande Smita N, BK Thel |
Association of dopaminergic pathway gene polymorphisms with chronic renal insufficiency among Asian Indians with type-2 diabetes. BMC genetics 2008 9 26. Prasad Pushplata, Kumar K M Prasanna, Ammini A C, Gupta Arvind, Gupta Rajeev, Thelma B |
Interleukin 10 promoter region polymorphisms in inflammatory bowel disease in Tunisian population. Inflammation research : official journal of the European Histamine Research Society ... [et al.] 2009 Mar 58 (3): 155-60. Marrakchi R, Moussa A, Ouerhani S, Bougatef K, Bouhaha R, Messai Y, Rouissi K, Khadimallah I, Khodjet-el-Khil H, Najar T, Benammar-Elgaaeid |
Clinical, molecular and geographical features of hereditary breast/ovarian cancer in latvia. Hereditary cancer in clinical practice 2010 3 3 (2): 71-6. Gardovskis Andris, Irmejs Arvids, Miklasevics Edvins, Borosenko Viktors, Bitina Marianna, Melbarde-Gorkusa Inga, Vanags Andrejs, Kurzawski Grzegorz, Suchy Janina, Górski Bohdan, Gardovskis Jan |
Detection of deafness-causing mutations in the Greek mitochondrial genome. Disease markers 2011 30 (6): 283-9. Kokotas Haris, Grigoriadou Maria, Korres George S, Ferekidou Elisabeth, Kandiloros Dimitrios, Korres Stavros, Petersen Michael |
Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathy. The Journal of molecular diagnostics : JMD 2012 Sep 14 (5): 518-24. Coto Eliecer, Reguero Julián R, Palacín María, Gómez Juan, Alonso Belén, Iglesias Sara, Martín María, Tavira Beatriz, Díaz-Molina Beatriz, Morales Carlos, Morís César, Rodríguez-Lambert José L, Corao Ana I, Díaz Marta, Alvarez Victor |
Allergy to betalactams and nucleotide-binding oligomerization domain (NOD) gene polymorphisms. Allergy 2013 Aug 68 (8): 1076-80. Bursztejn A C, Romano A, Guéant-Rodriguez R M, Cornejo J A, Oussalah A, Chery C, Gastin I, Gaeta F, Barbaud A, Blanca M, Guéant J |
NOD2 polymorphisms associated with cancer risk: a meta-analysis. PloS one 2014 9 (2): e89340. Liu Jingwei, He Caiyun, Xu Qian, Xing Chengzhong, Yuan Yu |
Functional Characterization of a Single Nucleotide Polymorphism in the 3' Untranslated Region of Sheep DLX3 Gene. PloS one 2015 10 (9): e0137135. Rong Enguang, Zhang Zhiwei, Qiao Shupei, Yang Hua, Yan Xiaohong, Li Hui, Wang Ni |
MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning. Journal of human genetics 2016 Mar . Zahorakova Daniela, Lelkova Petra, Gregor Vladimir, Magner Martin, Zeman Jiri, Martasek Pav |
Effects of genetic variations in the genes encoding NOD1 and NOD2 on type 2 diabetes mellitus and insulin resistance. Journal of clinical pharmacy and therapeutics 2017 Feb 42 (1): 98-102. Ozbayer C, Kurt H, Kebapci M N, Gunes H V, Colak E, Degirmenci |
Single-nucleotide polymorphisms in the genes of CES2, CDA and enzymatic activity of CDA for prediction of the efficacy of capecitabine-containing chemotherapy in patients with metastatic breast cancer. Pharmacological research 2017 Aug . Lam Siu W, van der Noort Vincent, van der Straaten Tahar, Honkoop Aafke H, Peters Godefridus J, Guchelaar Henk-Jan, Boven Ep |
[Inherited kidney stones: A nephrology center experience]. Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie 2019 9 29 (16): 962-973. Kaaroud H, Harzallah A, Sayhi M, Bacha M, Khadhar M, Goucha R, Bouzid K, Ayed H, Bouzouita A, Cherif M, Chebil M, Mrad R, Omezzine A, Jallouli M, Gargah T, Ben Hamida F, Ben Abdallah |
Association between EFHD2 gene polymorphisms and schizophrenia among the Han population in northern China. The Journal of international medical research 2020 6 48 (6): 300060520932801. Gao Meng, Zeng Kuo, Li Ya, Liu Yong-Ping, Xia Xi, Xu Feng-Ling, Yao Jun, Wang Bao-J |
Crohn's Disease Susceptibility and Onset Are Strongly Related to Three NOD2 Gene Haplotypes. Journal of clinical medicine 2021 9 10 (17): . Kaczmarek-Ry? Marta, Hryhorowicz Szymon Tytus, Lis Emilia, Banasiewicz Tomasz, Paszkowski Jacek, Borejsza-Wysocki Maciej, Walkowiak Jaros?aw, Cichy Wojciech, Krokowicz Piotr, Czkwianianc El?bieta, Hnatyszyn Andrzej, Krela-Ka?mierczak Iwona, Dobrowolska Agnieszka, S?omski Ryszard, P?awski Andrz |
Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes.
Progress in neuro-psychopharmacology & biological psychiatry 2021 Jul 110393. Wang Kesheng, Xu Chun, Smith Amanda, Xiao Danqing, Navia R Osvaldo, Lu Yongke, Xie Changchun, Piamjariyakul Ubolrat, |
Association of HLA-G 3'UTR polymorphisms and haplotypes with colorectal cancer susceptibility and prognosis. Human immunology 2021 Nov . Dhouioui Sabrine, Laaribi Ahmed-Baligh, Boujelbene Nadia, Jelassi Refka, Ben Salah Hamza, Bellali Hedia, Ouzari Hadda-Imene, Mezlini Amel, Zemni Inès, Chelbi Hanene, Zidi In |
The FADS1 genotypes modify the effect of linoleic acid-enriched diet on adipose tissue inflammation via pro-inflammatory eicosanoid metabolism. European journal of nutrition 2022 Jun . Vaittinen Maija, Lankinen Maria A, Käkelä Pirjo, Ågren Jyrki, Wheelock Craig E, Laakso Markku, Schwab Ursula, Pihlajamäki Jus |
Germline BRCA1 and BRCA2 mutations and the risk of bladder or kidney cancer in Poland. Hereditary cancer in clinical practice 2022 4 20 (1): 13. Z?owocka-Per?owska El?bieta, To?oczko-Grabarek Aleksandra, Narod Steven A, Lubi?ski J |
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